Bioburden Testing

Bioburden Testing

Bioburden Testing quantifies the population of viable microorganisms on a product, raw material or packaging prior to sterilisation. Per ISO 11737-1, it is the foundational input to sterilisation-cycle design, dose-setting for radiation sterilisation, and the periodic-revalidation framework for ETO and steam processes.

Our bioburden programme covers recovery-efficiency validation and neutralisation of antimicrobial residues — delivering defensible counts that feed directly into your sterility-assurance documentation.